LUMISCOPE MICRO 100— 510(k) K901726

Substantially Equivalent

Lumiscope Co., Inc.

FDA 510(k) clearance K901726 for LUMISCOPE MICRO 100, Substantially Equivalent on 1990-08-14. Applicant: Lumiscope Co., Inc.. Device class: 2.

Clearance details

Applicant: Lumiscope Co., Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1990-04-16
Decision date: 1990-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Edison, NJ, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.